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GB2037450A - Optical fibre - Google Patents

Optical fibre Download PDF

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Publication number
GB2037450A
GB2037450A GB7941259A GB7941259A GB2037450A GB 2037450 A GB2037450 A GB 2037450A GB 7941259 A GB7941259 A GB 7941259A GB 7941259 A GB7941259 A GB 7941259A GB 2037450 A GB2037450 A GB 2037450A
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United Kingdom
Prior art keywords
nylon
optical fiber
copolymer
layer
weight
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Granted
Application number
GB7941259A
Other versions
GB2037450B (en
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Daicel Corp
Original Assignee
Daicel Corp
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Daicel Corp filed Critical Daicel Corp
Publication of GB2037450A publication Critical patent/GB2037450A/en
Application granted granted Critical
Publication of GB2037450B publication Critical patent/GB2037450B/en
Expired legal-status Critical Current

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Classifications

    • GPHYSICS
    • G02OPTICS
    • G02BOPTICAL ELEMENTS, SYSTEMS OR APPARATUS
    • G02B6/00Light guides; Structural details of arrangements comprising light guides and other optical elements, e.g. couplings
    • G02B6/44Mechanical structures for providing tensile strength and external protection for fibres, e.g. optical transmission cables
    • G02B6/4401Optical cables
    • G02B6/4402Optical cables with one single optical waveguide
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B29WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
    • B29DPRODUCING PARTICULAR ARTICLES FROM PLASTICS OR FROM SUBSTANCES IN A PLASTIC STATE
    • B29D11/00Producing optical elements, e.g. lenses or prisms
    • B29D11/00663Production of light guides
    • CCHEMISTRY; METALLURGY
    • C03GLASS; MINERAL OR SLAG WOOL
    • C03CCHEMICAL COMPOSITION OF GLASSES, GLAZES OR VITREOUS ENAMELS; SURFACE TREATMENT OF GLASS; SURFACE TREATMENT OF FIBRES OR FILAMENTS MADE FROM GLASS, MINERALS OR SLAGS; JOINING GLASS TO GLASS OR OTHER MATERIALS
    • C03C25/00Surface treatment of fibres or filaments made from glass, minerals or slags
    • C03C25/10Coating
    • C03C25/104Coating to obtain optical fibres
    • C03C25/106Single coatings
    • CCHEMISTRY; METALLURGY
    • C03GLASS; MINERAL OR SLAG WOOL
    • C03CCHEMICAL COMPOSITION OF GLASSES, GLAZES OR VITREOUS ENAMELS; SURFACE TREATMENT OF GLASS; SURFACE TREATMENT OF FIBRES OR FILAMENTS MADE FROM GLASS, MINERALS OR SLAGS; JOINING GLASS TO GLASS OR OTHER MATERIALS
    • C03C25/00Surface treatment of fibres or filaments made from glass, minerals or slags
    • C03C25/10Coating
    • C03C25/24Coatings containing organic materials
    • C03C25/26Macromolecular compounds or prepolymers
    • C03C25/32Macromolecular compounds or prepolymers obtained otherwise than by reactions involving only carbon-to-carbon unsaturated bonds
    • C03C25/328Polyamides
    • GPHYSICS
    • G02OPTICS
    • G02BOPTICAL ELEMENTS, SYSTEMS OR APPARATUS
    • G02B6/00Light guides; Structural details of arrangements comprising light guides and other optical elements, e.g. couplings
    • G02B6/02Optical fibres with cladding with or without a coating
    • G02B6/02395Glass optical fibre with a protective coating, e.g. two layer polymer coating deposited directly on a silica cladding surface during fibre manufacture
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10TTECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T428/00Stock material or miscellaneous articles
    • Y10T428/29Coated or structually defined flake, particle, cell, strand, strand portion, rod, filament, macroscopic fiber or mass thereof
    • Y10T428/2904Staple length fiber
    • Y10T428/2907Staple length fiber with coating or impregnation

Landscapes

  • Chemical & Material Sciences (AREA)
  • Physics & Mathematics (AREA)
  • Engineering & Computer Science (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • General Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Optics & Photonics (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Physics & Mathematics (AREA)
  • Geochemistry & Mineralogy (AREA)
  • Materials Engineering (AREA)
  • General Life Sciences & Earth Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Manufacturing & Machinery (AREA)
  • Ophthalmology & Optometry (AREA)
  • Mechanical Engineering (AREA)
  • Surface Treatment Of Glass Fibres Or Filaments (AREA)
  • Optical Fibers, Optical Fiber Cores, And Optical Fiber Bundles (AREA)
  • Compositions Of Macromolecular Compounds (AREA)

Description

1
GB2 037 450A
1
SPECIFICATION
Optical fiber for optical transmission
5 The present invention relates to an optical fiber which possesses excellent transmission characteristics and has a high mechanical strength.
In the field of manufacture of optical fiber 10 cables for optical transmission, attempts have been made to attain a reinforcing effect by coating an optical fiber core with a plastics material or the like.
Fibers for optical communication are usually 15 made of a low-loss quartz or an optical glass, which are brittle materials. In order to make optical fiber cables for communication, therefore, studies have been directed toward reinforcing such cables to increase their mechani-20 cal strength by covering their cores with a plastics material or the like. The optical fiber cables of this type, however, have defects; for example breakage occurs in the cores of the optical fibers and degradation of the optical 25 transmission characteristics occurs when external pressures, impact or bending stresses are applied thereto. Therefore, polyethylene and nylon, which are crystalline thermoplastic resins having excellent mechanical and chemical 30 properties, have been proposed as materials for covering the cores of optical fibers. At present, nylon 12 is regarded as the most suitable covering material for optical fibers (see Japanese Patent Application Laid-Open 35 No. 17649/75 and U. S. Patent No. 3 980 390). Even a covering material composed of nylon 12, however, is not completely satisfactory and leaves room for improvement as described below.
40 In the case of conventional plastics materials, however, it is difficult to form a uniform coating having a thickness of from 100 to 500 n on an optical fiber core having a diameter of less than about 200 /*. Further-45 more, even if a uniform coating is formed, distortion is caused during the solidification process, resulting in an increase of the optical transmission loss. Accordingly, a product which is fully satisfactory for practical use has 50 not been obtained.
A plastics material preferred as the coating material for an optical fiber for optical transmission is required to have the following properties:
55 (1) In the coating step, a coating having a thickness of from 100 to 500 /i can be formed at a high efficiency on an optica! fiber core having a diameter of less than 200 /.i, which core is poor in mechanical strength; 60 (2) The distortion or strain in the coated product is low and hence, the optical transmission loss can be reduced;
(3) Quartz, optical glass or other materia! customarily used for making the optical fiber 65 core readily undergoes oxidation degrada ion or chemical degradation by contact with water or the like. A certain primer is coated on the optical fiber core to prevent such degradation. At a temperature higher than 200°C, this 70 primer is termally decomposed, resulting in reduction of the desired properties of the optical fiber core. Accordingly, the temperature for formation of the coating should be low.
75 (4) In the step of gathering or laying out optical fiber cables for transmission, the cables are required to have a good softness and a good slip characteristic. Furthermore, connection of the cables to each other should 80 be accomplished very simply and the optical transmission loss should be further reduced.
(5) The heat resistance stability in a longtime practical test for optical fiber cables (thermal degradation at 80° to 100°C and degra-85 dation by cooling-heating cycles), the dimensional stabilitthe moisture absorption stability, the stability of the mechanical properties and the stability against changes, with passing of time of the transmission loss in optical 90 fiber cables for optical transmission should be high.
As materials for meeting the above requirements, there can be mentioned nylon 12 and a nylon copolymer. However, these materials 95 are insufficient. For example, in the case of nylon 12, the degree of crystallization in the outer portion of the coating is different from that in the inner portion of the coating under some molding conditions, an internal strain is 100 caused by this difference of the degree of crystallization, and the optical transmission loss is increased by this internal strain. Since the crystallinity of the nylon copolymer is low, the abovementioned molding strain is main-105 tained at a very low level, but the elasticity is low and also the melting point is low. Accordingly, the nylon copolymer is inferior in the properties described in the above requirement (5).
110 Research was made with a view to obtaining a coating material that satisfies all of the requirements (1) to (5) set forth above. It was discovered that a mixture of (a) nylon 1 1 or nylon 12 and (b) a nylon copolymer, is very 115 excellent as the coating material. Based on this discovery, the present invention has been completed.
Figs. 1 and 2 relate to a blend of nylon 12 and nylon 12/nylon 6 copolymer according 120 to the invention. Fig. 1 is a graph showing the changes of the modulus of elasticity of the blend in respect of various temperatures and proportions of ingredients. Fig. 2 is a graph showing the changes of the melting heat of 125 the blend in respect of proportions of the ingredients.
The present invention will now be described in detail.
Nylon 12 and a nylon 12/nylon 6 co-130 polymer (a copolymer comprising 80 parts by
2
GB2 037 450A 2
weight of laurolactam and 20 parts by weight of caprolactam) are kneaded at various mixing ratios by a biaxial extruder, and the elasticity and crystallinity of the resulting mixtures are 5 examined.
The change of the elasticity depending on the mixing ratio of the nylon 1 2 and the copolymer of nylon 12 with nylon 6 is as shown in Fig. 1. The behavior is similar to 10 that commonly observed when a plastics material having a high elasticity is mixed with a plastics material having a low elasticity. However, the change of the heat of fusion (corresponding to the degree of crystalliza-15 tion), as measured by DSC (scanning calorimeter), depending on the mixing ratio, is very unusual and surprising. The present invention is based on this finding.
More specifically, the present invention has 20 been completed based on the finding that, as shown in Fig. 2, when the mixing ratio of nylon 12 to the nylon 12/nylon 6 copolymer is in the range of from 40/60 to 20/80 parts by weight, the degree of crystallization, as 25 indicated by the low value of melting heat, is remarkably low and hence, the internal strain is remarkably reduced.
Therefore, the present invention is characterized by the feature that when nylon 11 or 30 nylon 12 is mixed with a nylon copolymer, the crystallinity can be remarkably reduced without substantial degradation of the high elasticity possessed by nylon 11 or nylon 12, with the result being that the internal strain 35 can be remarkably reduced.
More specifically, in accordance with the present invention, there is provided an optical fiber for optical transmission in which a mixture comprising 5 to 95 parts by weight of 40 nylon 11 or nylon 12 and correspondingly 95 to 5 parts by weight of a nylon copolymer is used as a primary and/or secondary coating material for the optical fiber core for optical transmission.
45 The nylon 11 or nylon 12 that is used in the present invention has a relative viscosity of 1.5 to 2.4, as measured with respect to a 0.5% solution thereof in m-cresol. Nylon 11 or nylon 12 can be copolymerized with 50 another monomer copolymerizable with the nylon 11 or nylon 1 2, provided that the inherent crystallinity of nylon 11 or nylon 1 2 is not substantially affected. In this case, the content of nylon 11 or nylon 12 should be 55 higher than 90 wt. %.
As the nylon copolymer, there can be used any of the semicrystalline and amorphous nylon copolymers, provided that it is compatible with nylon 11 or nylon 12.
60 Nylon monomers to form the nylon copolymer used in the invention include lactams having 4 to 16 carbon atoms, tj-amino-car-boxylic acis having 4 to 16 carbon atoms and salts of alkylene diamines having 4 to 16 65 carbon atoms and alkylene dicarboxylic acids having 4 to 1 6 carbon atoms. Preferred monomers are caprolactam, capryl lactam and laurolactam as the lactam; co-amino-pelargonic acid and w-amino-undecanoic acid as the «-smino-carboxylic acid; and hexamethylene diamine sebacate, hexamethylene diamine adi-pate, hexamethylene diamine dodecane-dicar-boxylate, and hexamethylene diamine tride-cane-dicarboxylate as the salt. As to other salts, there can be also used salts of sebacic acid, adipic acid, dodecane dicarboxylic acid or tridecane dicarboxylic acid with decamethy-lene diamine, tridecanediamine or 2,2,4- or 2,4,4,-trimethyl hexadiamine.
The nylon copolymer is prepared by conventional polymerization of two or more kinds of monomers.
The most preferable nylon copolymer contains ^-amino-undecanoic acid or laurolactam as one monomer.
It is further preferred that the nylon copolymer has a melting point of from 90°C to 170°C. The melting point is measured as being the temperature where the maximum absorption of heat appears when the nylon copolymer is heated at a rate of 16°C/min., as measured by a differential scanning calorimeter.
In this preferred nylon copolymer, it is preferred that the content of w-amino-undeca-noic acid or laurolactam in the nylon copolymer is from 20 to 90 wt. %, preferably from 30 to 80 wt. %.
The mixing ratio betweeng (1) nylon 11 or nylon 12 and (2) the nylon copolymer, should be determined depending on the atmosphere and the field in which the optical transmission fiber is to be used. Ordinarily, the mixing ratio of nylon 11 or nylon 12 to the copolymer nylon is in the range of from 95/5 to 5/95, preferably about 10/90 to 80/20.
In producing the fiber for optical communications according to the present invention, the covering layer of the blend of nylon 11 or 12 and the nylon copolymer can be formed on the core of the optical fiber by any known method of forming the covering layer. The most suitable method, however, is to melt the resin composition and to cover the core of the optical fiber by extruding the resin composition onto the core. Namely, the resin, composition is melted by means of a screw extruder and is coated on the core by way of a drawing method (inclusive of vacuum lining method), or the resin composition is melted by any suitable method and is extruded by means of a gear pump to apply it to the core.
The thus obtained coated fiber for optical communications may then be covered on its outer surface with a protective layer whereby to make an optical fiber cable. Such a cable can be manufactured in the same manner as the conventional optical fiber cables. A plurality of the coated optical fibers may be formed into one cable by enveloping same with a
70
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130
3
GB2 037 450A
3
sheath of a thermoplastic resin.
As described above, the fiber for optical communications according to the invention preferably has a special coating layer on the 5 surface. A plurality of such optical fibers coated with the nylon blend according to the invention may be bundled and the bundle is coated with a thermoplastic resin. Practical embodiments of the invention can include an 10 optical fiber having thereon at least one coating layer of the nylon blend according to the invention and at least one coating layer of another resin such as those listed below. It is furthermore added that the coating layer is 15 preferred to be either a single or a double layer. In the case of the double layer, the outer layer may be composed of the nylon blend according to the invention and the inner layer can be composed of a resin different 20 from that of the outer layer. The resin used as a basic ingredient of the resin composition used herein to make the other layer can be of any suitable type such as thermoplastic resins, thermosetting resins and the like and, from 25 the viewpoint of the adhesion to the glass fiber, suitable resins for the other layer include, for example, polyethylene, vinyl resins such as polyvinyl chloride, polyester, polyam-ide, polyacetal, polyvinylacetal, polysulfone, 30 polyurethane, polyether, polyesterimide, poly-amideimide, polyimide, polyacrylate, polyviny-lacetate, ethylenevinylacetate copolymer, ethy-lene-acrylic acid copolymer, epoxy resin, phenol resin, resorcinol resin, unsaturated polyes-35 ter resin, urea resin, furan resin, silicone resin, alkyd resin, melamine resin, diallylphthalate resin, etc or derivatives thereof.
One of the practical embodiments of the invention is a fiber having two superposed 40 coating layers composed of silicone resin and the nylon blend according to the invention, disposed respectively from the inside to the outside.
The low-loss optical fiber core to be used in 45 the invention can include any of the conventional ones, such as those of the glass-clad type, the self-focusing type and the single material type.
The present invention will now be further 50 described with reference to the following illustrative Examples.
Example 1
A mixture comprising 30 parts by weight of 55 nylon 12 and 70 parts by weight of a nylon 12/nylon 6 copolymer (80/20), having a melting point of 155°C, was kneaded by a biaxial extruder and was extrusion-coated as a layer having a thickness of 300 |iona clad-60 type optical fiber core of quartz glass having a diameter of 200 [i from a drawdown die, by using an extruding machine for nylon having a screw diameter of 40 mm. An optical transmission fiber was prepared by using the thus-65 coated optical fiber. The resulting optical transmission fiber was very flexible and the thickness deviation of the coating having a thickness of 300 /i was within ± 30 ju, and the dimensional stability was very good. 70 The optical transmission loss of the thus-obtained optical fiber was measured after 24 hours had passed from the preparation thereof. It was found that the optical transmission loss was 5 dB/Km. This value was quite 75 the same as the value of the transmission loss of the optical fiber core and the transmission loss was not increased at all by the above-mentioned plastic coating. Thus, it was confirmed that the mixture used in this Example 80 is a very excellent coating material. Furthermore, since the elasticity of the mixture was higher than the elasticity of the nylon 1 2/nylon 6 copolymer, the terminal treatment could be accomplished very easily.
85
Example 2
An optical fiber for optical transmission was prepared by coating a mixture of 70 parts by weight of a nylon 12/nylon 6 copolymer 90 (laurolactam/caprolactam = 95/5) and 30 parts by weight of a nylon 12/nylon 6 copolymer (80/20) was coated on an optical fiber core having a diameter of 1 50 /j and which was coated with a silicone rubber coating of 95 100 ]U in thickness, according to the same procedures as described in Example 1. The transmission loss of the thus-obtained optical transmission fiber was measured after 24 hours had passed from the preparation 100 thereof. It was found that the transmission loss was 6 dB/Km and the increase of the transmission loss due to formation of the nylon mixture coating was only 1 dB/Km. The optical transmission fiber was very excel-105 lent in the abrasion resistance and mechanical characteristics such as the bending property.
Example 3
An optical fiber for optical transmission was 110 prepared by coating a mixture of 50 parts by weight of nylon 11 and 50 parts by weight of a nylon 6/nylon 6,6/nyIon 12 copolymer (caprolactam/hexamethylene adipate/lauro-lactam = 30/30/40), having a melting 115 point of 106°C, on an optical fiber core having a diameter of 200 /x, according to the same procedure as described in Example 1. The transmission loss of the thus-formed optical transmission fiber was measured after 24 1 20 hours had passed from the preparation thereof. It was found that the transmission loss was 8 dB/Km and the increase of the transmission loss owing to the coating of the nylon mixture was only 3 dB/Km.
125

Claims (1)

1. An optical fiber for optical transmission comprising a core of optical fiber for optical transmission coated with a layer of a mixture 130 consisting essentially of from 5 to 95 percent
4
GB2 037 450A 4
by weight of nylon 11 or nylon 1 2 and correspondingly from 95 to 5 percent by weight of nylon copolymer.
2. An optical fiber as claimed in claim 1 in 5 which said mixture contains from about 10 to about 80 percent by weight of nylon 11 or nylon 12 and correspondingly from about 90 to about 20 percent by weight of said nylon compolymer.
10 3. An optical fiber as claimed in claim 1 in I
which said core has a diameter of about 200 microns or less, and the thickness of said layer is from about 100 to about 500 microns.
15 4. An optical fiber as claimed in claim 1 or claim 3 in which said nylon copolymer is amorphous or semi-crystalline and is compatible with said nylon 11 or nylon 12.
5. An optical fiber as claimed in claim 4 in 20 which said nylon copolymer has a melting point of from about 90° to about 170°C.
6. An optical fiber as claimed in claim 5 in which said nylon copolymer is a copolymer of two or more different polyamide-forming mon-
25 omers selected from lactams having 4 to 1 6 carbon atoms, w-amino-carboxylic acids having 4 to 16 carbon atoms and salts of alkylene diamines having 4 to 16 carbon atoms and alkylene dicarboxylic acids having 4 to 16 30 carbon atoms.
7. An optical fiber as claimed in claim 6 in which said nylon copolymer contains from 20 to 90 percent by weight of co-amino unde-canoic acid or laurolactam.
35 8. An optical fiber as claimed in claim 6 in which said nylon copolymer contains from 30 to 80 percent by weight of w-amino undeca-noic acid or laurolactam.
9. An optical fiber as claimed in any one 40 of claims 1 to 8 which is also coated with one or more additional layers of a thermoplastic or thermosetting resin different from said mixture.
10. An optical fiber as claimed in claim 9 45 in which said additional layer is an inner layer and said layer of said mixture is an outer layer on said core.
11. An optical fiber as claimed in claim
10 in which said core is coated with an inner 50 layer of silicone resin and said coating of said mixture is an outer layer coated on said inner layer.
12. An optical fiber as claimed in any one of claims 1 to 11 in which said nylon 11 or 4
55 nylon 12 have a relative viscosity in the range of from 1.5 to 2.4.
13. An optical fiber as claimed in claim 1 and substantially as hereinbefore described with reference to any one of the Examples.
Printed for Her Majesty's Stationery Office by Burgess & Son (Abingdon) Ltd.—1980.
Published at The Patent Office, 25 Southampton Buildings,
London, WC2A 1AY, from which copies may be obtained.
GB7941259A 1978-11-30 1979-11-29 Optical fibre Expired GB2037450B (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP14821078A JPS5595902A (en) 1978-11-30 1978-11-30 Optical fiber for transmission

Publications (2)

Publication Number Publication Date
GB2037450A true GB2037450A (en) 1980-07-09
GB2037450B GB2037450B (en) 1983-05-11

Family

ID=15447721

Family Applications (1)

Application Number Title Priority Date Filing Date
GB7941259A Expired GB2037450B (en) 1978-11-30 1979-11-29 Optical fibre

Country Status (5)

Country Link
US (1) US4274709A (en)
JP (1) JPS5595902A (en)
DE (1) DE2947942C2 (en)
FR (1) FR2443073A1 (en)
GB (1) GB2037450B (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB2198258A (en) * 1986-11-17 1988-06-08 Inventa Ag Optical wave-guides
US6842575B2 (en) 1999-11-29 2005-01-11 Mitsubishi Rayon Co., Ltd. Optical fiber cord and optical fiber cord with a plug

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* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS57191603A (en) * 1981-05-21 1982-11-25 Kokusai Denshin Denwa Co Ltd <Kdd> Optical fiber unit for submarine cable
FR2533709B1 (en) * 1982-09-23 1985-10-18 Commissariat Energie Atomique OPTICAL FIBERS IN PLASTIC MATERIAL, ESPECIALLY SPARKLING AND THEIR MANUFACTURING METHOD
JPS5979803U (en) * 1982-11-19 1984-05-30 古河電気工業株式会社 optical fiber core
DE3926604A1 (en) * 1989-08-11 1991-02-14 Hoechst Ag POLYIMIDE WAVE GUIDE AS OPTICAL SENSORS
US5567219A (en) * 1994-07-20 1996-10-22 Galileo Electro-Optics Corporation Polyimide coated heavy metal fluoride glass fiber and method of manufacture
US5714196A (en) * 1994-07-20 1998-02-03 Galileo Corporation Method of forming a strippable polyimide coating for an optical fiber
AU2001294554A1 (en) 2000-09-15 2002-03-26 First Quality Fibers, Inc. Apparatus for manufacturing optical fiber made of semi-crystalline polymer
US8369673B2 (en) * 2010-06-08 2013-02-05 Bluefin Robotics Corporation Ocean deployable biodegradable optical fiber cable
US8574385B2 (en) * 2010-07-20 2013-11-05 O Fs Fitfl, Llc Attaching a communication line to a target surface on or inside of a building
AU2015417227A1 (en) * 2015-12-16 2018-07-19 Politecnico Di Milano Optical fibre with enhanced high temperature resistance
CN117925086A (en) * 2024-01-15 2024-04-26 万华化学集团股份有限公司 High-cohesiveness nylon 12 powder coating and preparation method and application thereof

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GB1143689A (en) * 1900-01-01
JPS4927233A (en) * 1972-07-03 1974-03-11
DE2512312C2 (en) * 1974-03-20 1984-09-13 Sumitomo Electric Industries, Ltd., Osaka Process for coating an optical fiber glass fiber
US4167305A (en) * 1974-06-17 1979-09-11 Sumitomo Electric Industries Ltd. Optical transmission fiber
DE2456069A1 (en) * 1974-11-25 1976-05-26 Siemens Ag Conductor for optical fibre cable - allowing improved handling and identification during manufacture and assembly
US4072400A (en) * 1975-07-07 1978-02-07 Corning Glass Works Buffered optical waveguide fiber
GB1570624A (en) * 1975-12-11 1980-07-02 Western Electric Co Optical fibre transmission arrangements
US4105284A (en) * 1976-05-10 1978-08-08 Corning Glass Works Buffered optical waveguide fiber
JPS52143844A (en) * 1976-05-26 1977-11-30 Nippon Telegr & Teleph Corp <Ntt> Glass fibres for photo communication
US4125644A (en) * 1977-05-11 1978-11-14 W. R. Grace & Co. Radiation cured coatings for fiber optics
DE2724155A1 (en) * 1977-05-27 1978-12-07 Siemens Ag MESSAGE CABLES WITH FIBER OPTIC FIBER WAVE GUIDES
GB1524316A (en) * 1977-06-10 1978-09-13 Gen Electric Co Ltd Optical fibre waveguides
DE2729648A1 (en) * 1977-06-30 1979-01-04 Siemens Ag TENSION-RESISTANT LIGHT WAVE GUIDE
JPS54134450A (en) * 1978-04-10 1979-10-18 Daicel Ltd Fiber for photoocommunication

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB2198258A (en) * 1986-11-17 1988-06-08 Inventa Ag Optical wave-guides
GB2198258B (en) * 1986-11-17 1990-08-22 Inventa Ag Optical wave-guides having polyamide mixture cladding.
US6842575B2 (en) 1999-11-29 2005-01-11 Mitsubishi Rayon Co., Ltd. Optical fiber cord and optical fiber cord with a plug

Also Published As

Publication number Publication date
JPS5595902A (en) 1980-07-21
DE2947942C2 (en) 1983-02-03
FR2443073B1 (en) 1983-05-27
FR2443073A1 (en) 1980-06-27
GB2037450B (en) 1983-05-11
US4274709A (en) 1981-06-23
DE2947942A1 (en) 1980-06-04

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PCNP Patent ceased through non-payment of renewal fee
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